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Bacterioclastic Action of a Bis-Quaternary Ammonium Compound against Escherichia coli

机译:双季铵化合物对大肠杆菌的抗菌作用。

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It has been reported that the bactericidal action of bis-quaternary ammonium compounds (bis-QACs) is little influenced by the molecular hydrophobicity of the drug or environmenta! conditions such as temperature or pH. In order to clarify the mode of bactericidal action of bis-QACs against Escherichia co/i, the bacterioclastic action of 4,4'-(1,6-hexamethylenedithio) bis (1-octylpyridinium bromide) (4DTBP-6,8) was investigated. It was suggested that 4DTBP-6.8, which invaded the bacterial ceil, inducedthe leakage of ATP and the inhibition of the respiratory enzymes, and resulted in cell death. Subsequently, over 2 μg /ml of 4DTBP-6,8 caused an increase in the turbidity of the cell suspension, and the bactericidal activity of 4DTBP-6,8 was extremelyincreased with the increase of its concentration (over 2 μg/ml). It indicated that 4DTBP-6,8 has an ability to induce a rapid and abundant secretion of the turbid materials from the ceils and that such bacterioclastic ability is connected to its potentbactericidal activity, in addition, it was suggested that the first stage of bacteriociastic action of 4DTBP-6,8 was the leakage of magnesium ion (Mg~(2+)), and the leakage of the outer membrane pore protein E and lipopolysaccharides followed it. The formation of blebs and holes on the bacterial cell surface was revealed by scanning electron microscopic investigation. Transmission electron micrographs of the cells treated with 4DTBP-6,8 showed the destruction of peptidoglycan and large missing portionsof intercellular materials. Judging from these results, as the mechanism of the bacterioclastic action of bis-QACs, it is suggested that the cationic parts of bis-QACs electrically interact with the cationic parts of Mg~(2+) on the bacterial surface, then bis-QACs invade the cell membrane by displacement reaction with Mg~(2+), and rapidly destroy the bacterial cell surface structure.
机译:据报道,双季铵化合物(bis-QACs)的杀菌作用几乎不受药物或环境分子疏水性的影响。温度或pH等条件。为了阐明bis-QAC对大肠杆菌的杀菌作用模式,对4,4'-(1,6-六亚甲基二硫代)双(1-辛基溴化吡啶鎓)(4DTBP-6,8)的杀菌作用进行了研究。调查。提示侵入细菌细胞的4DTBP-6.8诱导ATP的泄漏和呼吸酶的抑制,导致细胞死亡。随后,超过2μg/ ml的4DTBP-6,8导致细胞悬浮液的浊度增加,并且4DTBP-6,8的杀菌活性随其浓度的增加而大大增加(超过2μg/ ml)。这表明4DTBP-6,8具有诱导细胞快速大量分泌浑浊物质的能力,并且这种细菌破灭能力与其潜在的杀菌活性有关,此外,还表明细菌杀菌作用的第一阶段4DTBP-6,8的渗漏是镁离子(Mg〜(2+))的泄漏,其次是膜外孔蛋白E和脂多糖的泄漏。通过扫描电子显微镜研究揭示细菌细胞表面上的气泡和孔的形成。用4DTBP-6,8处理的细胞的透射电子显微照片显示肽聚糖的破坏和细胞间物质的大量缺失部分。从这些结果来看,作为bis-QACs的破细菌作用机理,建议bis-QACs的阳离子部分与细菌表面Mg〜(2+)的阳离子部分发生电相互作用,然后使bis-QACs发生相互作用。通过与Mg〜(2+)的置换反应侵入细胞膜,迅速破坏细菌细胞的表面结构。

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